Testosterone does not mediate the correlation between dietary inflammation and serum klotho levels among males: insights from NHANES database.

ABSTRACT

Introduction: Serum Klotho (S-Klotho) is a transmembrane protein holds pivotal roles in anti-aging. The Dietary Inflammation Index (DII), a meticulously dietary tool, quantifies the inflammatory potential of an individual's diet. The existing research strongly suggests that a low DII diet plays a significant role in delaying aging and reducing aging-related symptoms in males. Testosterone could potentially act as a mediating intermediary between DII and S-Klotho. However, this aspect remains unexplored. This study aims to investigate the potential causal link of testosterone between DII and S-Klotho in males. Methods: We utilized data from National Health and Nutrition Examination Survey (NHANES) which focused on male participants from 2013-2016. Mediation analyses were used to investigate the effects of testosterone (TT), free testosterone (FT), and free androgen index (FAI) on the DII-S-Klotho relationship, using three modes adjusting for covariates. Results: Mediation analysis unveiled a significant inverse correlation between DII and S-Klotho levels (model 1 c = -14.78, p = 0.046). The interaction between DII and S-Klotho was modulated by TT in model 1 (ab = -1.36; 95% CI -5.59, -0.55; p = 0.008), but lost significance after adjustments (model 2 ab = -0.39; 95% CI -4.15, 1.66; p = 0.378; model 3 ab = -0.59; 95% CI -4.08, 2.15; p = 0.442). For FT, the mediating impact was not statistically significant (model 1 ab = 0.43; 95% CI -0.51, 5.44; p = 0.188; model 2 ab = 0.72; 95% CI -0.26, 5.91; p = 0.136; model 3 ab = 0.84; 95% CI -0.02, 8.06; p = 0.056). Conversely, FAI consistently influenced the DII-S-Klotho relationship (model 1 ab = 2.39; 95% CI 0.69, 9.42; p = 0.002), maintaining significance after adjustments (model 2 ab = 3.2; 95% CI 0.98, 11.72; p = 0.004; model 3 ab = 3.15; 95% CI 0.89, 14.51; p = 0.026). Discussion: This study observed no mediating influence of TT or FT on the correlation between DII and S-Klotho after covariate control. Remarkably, FAI continued to significantly mediate the DII-S-Klotho connection even following covariate adjustment, although its significance in males warrants careful consideration.